Alcon AcrySof®

GUDID 00380659909467

AcrySof® IQ Toric IOL Calculator

Alcon Laboratories, Inc.

Intraocular lens web-based calculator software
Primary Device ID00380659909467
NIH Device Record Key0d3a82fc-6ed1-4969-8950-0c87bab08972
Commercial Distribution StatusIn Commercial Distribution
Brand NameAlcon AcrySof®
Version Model NumberVersion 3
Company DUNS008018525
Company NameAlcon Laboratories, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+18008625266
Emailweb.masterus@alcon.com
Phone+18008625266
Emailweb.masterus@alcon.com
Phone+18008625266
Emailweb.masterus@alcon.com
Phone+18008625266
Emailweb.masterus@alcon.com
Phone+18008625266
Emailweb.masterus@alcon.com
Phone+18008625266
Emailweb.masterus@alcon.com
Phone+18008625266
Emailweb.masterus@alcon.com
Phone+18008625266
Emailweb.masterus@alcon.com
Phone+18008625266
Emailweb.masterus@alcon.com
Phone+18008625266
Emailweb.masterus@alcon.com
Phone+18008625266
Emailweb.masterus@alcon.com
Phone+18008625266
Emailweb.masterus@alcon.com
Phone+18008625266
Emailweb.masterus@alcon.com
Phone+18008625266
Emailweb.masterus@alcon.com
Phone+18008625266
Emailweb.masterus@alcon.com
Phone+18008625266
Emailweb.masterus@alcon.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100380659909467 [Primary]

FDA Product Code

HQLintraocular lens

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-06-07
Device Publish Date2016-12-13

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